Arcuate fixation member

ABSTRACT

Arcuate fixation members with varying configurations and/or features are provided, along with additional components for use therewith in provided intervertebral implants. The arcuate fixation members may be of different lengths, cross sectional geometries, and/or cross sectional areas. Applications of intervertebral implants utilizing arcuate fixation members are particularly suitable when a linear line-of-approach for delivering fixation members is undesirable.

CROSS-REFERENCE TO RELATED APPLICATIONS

This patent application is a continuation-in-part of and claims priority to U.S. patent application Ser. No. 12/761,101, filed Apr. 15, 2010. U.S. patent application Ser. No. 12/761,101 claims priority to U.S. provisional patent application No. 61/169,461, filed Apr. 15, 2009. The disclosures of U.S. patent application Ser. No. 12/761,101 and U.S. provisional patent application No. 61/169,461 are hereby incorporated by reference as if set forth in their entireties herein.

TECHNICAL FIELD

The present disclosure relates generally to orthopedics, and in particular relates to fixation systems, intervertebral implants, and associated surgical methods and procedures for using same.

BACKGROUND

Spinal fixation systems such as pedicle screw and rod constructs are commonly used to promote fusion between intervertebral bodies. The insertion of pedicle screws typically requires a linear “line-of-approach” trajectory that is aligned with the longitudinal axis of the screw, in order to accommodate the access and delivery instruments. Similarly, anchors such as bone screws may be used to directly fix intervertebral implants to vertebral bodies, typically requiring the insertion of several screws at unique angles oblique to the sagittal and/or transverse plane, and thus multiple lines-of-approach. However, in a variety of surgical situations, achieving a desired trajectory for screw insertion can be difficult due to the patient's anatomy obstructing a linear line-of-approach. For example, medially-directed placement of pedicle screws into the sacrum is desirable to prevent screw loosening and/or pullout, but can be prohibited due to the iliac crest obstructing the linear line-of-approach.

SUMMARY

In accordance with one embodiment, a bone fixation member configured to be inserted in a vertebral body includes a fixation body having opposing proximal and distal ends and a curved intermediate portion extending between the proximal and distal ends. A tip configured to cut into bone is defined at the distal end. A guidance member is disposed at the tip and extends toward the proximal end of the body. The guidance member is configured to guide the tip along an insertion trajectory as the fixation member is inserted into a vertebral body.

The bone fixation member can be used with an intervertebral implant that includes a spacer body that is configured to be implanted into an intervertebral space. The spacer body has an outer wall that defines at least a first aperture extending into the spacer body. The intervertebral implant also includes an insert that defines a plate. The insert is configured to be coupled to the spacer body such that the insert and the outer wall of the spacer body define a second aperture therebetween.

An alternative intervertebral implant that can be used with the bone fixation member includes a spacer body that has upper and lower plates and an outer wall extending between the upper and lower plates. The spacer body has a plurality of apertures extending through each of the upper and lower plates. The intervertebral implant also includes an insert that defines a plate. The insert is configured to be coupled to the spacer body such that the insert is disposed opposite at least a portion of the outer wall.

BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing summary, as well as the following detailed description of the preferred embodiments of the application, will be better understood when read in conjunction with the appended drawings. For the purposes of illustrating the arcuate fixation member and intervertebral implants for use therewith, there are shown in the drawings preferred embodiments. It should be understood, however, that the instant application is not limited to the precise arrangements and/or instrumentalities illustrated in the drawings, in which:

FIG. 1A is a side elevation view of an arcuate fixation member constructed in accordance with an embodiment;

FIG. 1B is a perspective view of the arcuate fixation member illustrated in FIG. 1A;

FIG. 2A is a top elevation view of an intervertebral implant spacer for use with arcuate fixation members, constructed in accordance with an embodiment;

FIG. 2B is a front elevation view of the intervertebral implant spacer illustrated in FIG. 2A;

FIG. 2C is a side elevation view of the intervertebral implant spacer illustrated in FIG. 2A;

FIG. 3A is a front elevation view of an insert plate for use with the intervertebral implant spacer illustrated in FIGS. 2A-C;

FIG. 3B is a top elevation view of the insert plate illustrated in FIG. 3A;

FIG. 4A is a front elevation view of a blocking plate for use with the insert plate illustrated in FIGS. 3A-B;

FIG. 4B is a top elevation view of the blocking plate illustrated in FIG. 4A;

FIG. 4C is a front elevation view of a blocking plate similar to the blocking plate illustrated in FIG. 4A, but constructed in accordance with an alternative embodiment;

FIG. 5 is a side elevation view of a locking screw for use with the insert plate and blocking plate illustrated in FIGS. 3A-B and 4A-B, respectively;

FIG. 6A is an exploded view of an intervertebral implant assembly constructed from the intervertebral implant system components illustrated in FIGS. 1A-5;

FIG. 6B is a perspective view of the intervertebral implant assembly illustrated in FIG. 6A, in an assembled configuration;

FIG. 6C is a side elevation view of the intervertebral implant assembly illustrated in FIG. 6B, inserted into an intervertebral space;

FIG. 7A is a side elevation view of an arcuate fixation member constructed in accordance with an alternative embodiment;

FIG. 7B is a front perspective view of the arcuate fixation member illustrated in FIG. 7A;

FIG. 7C is a rear elevation view of the arcuate fixation member illustrated in FIG. 7A;

FIG. 7D is a rear perspective view of the arcuate fixation member illustrated in FIG. 7A;

FIG. 7E is a front perspective view of a portion of the arcuate fixation member in FIG. 7A, showing a guidance member;

FIG. 7F is a rear perspective view of the portion of the arcuate fixation member in FIG. 7E;

FIG. 7G is a top elevation view of the arcuate fixation member illustrated in FIG. 7A;

FIG. 7H is a sectional front elevation view of the arcuate fixation member illustrated in FIG. 7G, taken along line 7H-7H;

FIG. 7I is a rear elevation view of an arcuate fixation member similar to the arcuate fixation member illustrated in FIG. 7A, but constructed in accordance with an alternative embodiment;

FIG. 7J is a rear perspective view of the arcuate fixation member illustrated in FIG. 7I;

FIG. 8A is a top elevation view of an intervertebral implant spacer for use with arcuate fixation members, constructed in accordance with an alternative embodiment;

FIG. 8B is a perspective view of the intervertebral implant spacer illustrated in FIG. 8A;

FIG. 8C is a front elevation view of the intervertebral implant spacer illustrated in FIG. 8A;

FIG. 8D is a side elevation view of the intervertebral implant spacer illustrated in FIG. 8A;

FIG. 9A is a top elevation view of an intervertebral implant spacer for use with arcuate fixation members, constructed in accordance with another alternative embodiment;

FIG. 9B is a perspective view of the intervertebral implant spacer illustrated in FIG. 9A;

FIG. 9C is a front elevation view of the intervertebral implant spacer illustrated in FIG. 9A;

FIG. 9D is a side elevation view of the intervertebral implant spacer illustrated in FIG. 9A;

FIG. 10A is a top elevation view of an insert plate for use with the intervertebral implant spacers illustrated in FIGS. 8A-D and 9A-D;

FIG. 10B is a front elevation view of the insert plate illustrated in FIG. 10A;

FIG. 10C is a rear elevation view of the insert plate illustrated in FIG. 10A;

FIG. 10D is a perspective view of the insert plate illustrated in FIG. 10A;

FIG. 10E is a top elevation view of the insert plate illustrated in FIG. 10A, constructed in accordance with an alternative embodiment;

FIG. 10F is a top elevation view of the insert plate illustrated in FIG. 10A, constructed in accordance with another alternative embodiment;

FIG. 11A is a top elevation view of an intervertebral implant constructed with an alternative embodiment of the intervertebral implant spacer illustrated in FIGS. 8A-D and the insert plate illustrated in FIGS. 10A-D;

FIG. 11B is a sectional elevation view of the intervertebral implant illustrated in FIG. 11A, taken along line 11B-11B;

FIG. 12A is a top elevation view of the intervertebral implant illustrated in FIG. 11A, constructed in accordance with an alternative embodiment;

FIG. 12B is a top elevation view of the intervertebral implant illustrated in FIG. 11A, constructed in accordance with another alternative embodiment;

FIG. 12C is a top elevation view of the intervertebral implant illustrated in FIG. 11A, constructed in accordance with still another alternative embodiment;

FIG. 13A is a side elevation view of an intervertebral implant constructed in accordance with an embodiment; and

FIG. 13B is a side elevation view of the intervertebral implant illustrated in FIG. 12A, constructed in accordance with another embodiment.

FIG. 14A is an exploded view of an intervertebral implant constructed from the intervertebral implant system components illustrated in FIGS. 7A-8D and 10A-D; and

FIG. 14B is a perspective view of the intervertebral implant illustrated in FIG. 14A, in an assembled configuration.

DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

Certain terminology is used in the following description for convenience only and is not limiting. The words “right”, “left”, “top” and “bottom” designate directions in the drawings to which reference is made. The words “inwardly” and “outwardly” refer to directions toward and away from, respectively, the geometric center of the device and designated parts thereof. The words, “anterior”, “posterior”, “superior”, “inferior”, “lateral”, “medial”, “sagittal”, “axial”, “coronal,” “cranial,” “caudal” and related words and/or phrases designate preferred positions and orientations in the human body to which reference is made and are not meant to be limiting.

The words “arcuate” and “curved” as used herein refer generally to the varying physical geometry of an object along an axis coincident to the object, for example the deviation from straightness of the body of an arcuate fixation member along a central longitudinal axis defined within the body of the object between its proximal and distal ends. Generally, with reference to a straight axis projected from a first end of such an object, as distance from the first end of the object increases along the central longitudinal axis of the object, distance between the central longitudinal axis of the object and the straight axis increases more or less continuously, so that the body of the object defined along its central longitudinal axis takes on a curved or arcuate shape. The resulting curvature of the central longitudinal axis may exhibit a constant or uniform radius with respect to a point in space defined remotely from the body of the object. Alternatively, a non-uniform or varying radius of curvature may be defined. The curvature of the body of the object defined by the longitudinal axis may also vary in direction with respect to a Cartesian coordinate system. The curvature may be uniformly distributed along the body of the object, for example between the proximal and distal ends of the object, or may be localized within one or more distinct segments of the body of the object. The curvature of the object may be significantly smooth and continuous along its central longitudinal axis, may be defined by a series of straight interconnected segments where each successive segment defines an increasing angle between the central longitudinal axis of the body of the object and the straight axis, or any combination thereof.

The words “vertebral body” as used herein should be interpreted broadly to include all the bones and bony structures found within and in the immediate proximity of the human spinal system, including but not limited to those found in the cervical region, the thoracic region, the lumbar region, and the sacral curve region.

The terminology intended to be non-limiting includes the above-listed words, derivatives thereof and words of similar import.

Referring initially to FIGS. 1A-6C, example embodiments of components of an intervertebral implant system 100 comprising a bone fixation member which can define an arcuate fixation member 12C as illustrated, an intervertebral implant spacer 108, an insert plate 116, a blocking plate 132, and a locking screw 138 are illustrated. Applications of the intervertebral implant system 100 could include, but are not limited to, fixation of the endplate components of a total disc replacement to vertebral bodies, direct fixation of an intervertebral implant to vertebral bodies, fixation into osteoporotic bone, and the like. The use of the systems and/or methods utilizing arcuate fixation members disclosed herein are particularly suitable when a linear line-of-approach for delivering a fixation member is undesirable. It should be noted that the physical characteristics of the arcuate fixation members disclosed herein may cause them to be alternately described as curved fixation members, arcuate or curved blades, arcuate or curved pins, arcuate or curved nails, or other terms of similar descriptive import.

As will become appreciated from the description below, one or more fixation members 12C may be utilized to securely anchor an assembled configuration of intervertebral implant system 100 within an intervertebral space between adjacent vertebral bodies. Unless otherwise indicated, the intervertebral implant system 100 and its components can be manufactured from any suitable biocompatible material known in the art including but not limited to titanium, titanium alloy such as TAN, commercially pure titanium, stainless steel, tantalum, polymers such as polyether ether ketone (PEEK), reinforced plastics, allograft bone, and the like.

Referring now to FIGS. 1A-B, the arcuate fixation member 12C includes a body 102 defining a proximal end 102 a and a distal end 102 b opposite the proximal end. The distal end 102 b may comprise a tip 104 configured to cut into underlying structure or bone. The body 102 may further define an intermediate portion between the proximal end 102 a and the distal end 102 b that is curved along a central curved axis L1. In an embodiment, the intermediate portion is curved along substantially the entire length of the body 102 between the proximal end 102 a and the distal end 102 b. Alternatively, one or more distinct portions of the intermediate portion between the proximal end 102 a and the distal end 102 b may be curved (not shown).

In the illustrated embodiment, the intermediate portion is curved along the central curved axis L1 in accordance with a uniform radius of curvature R1. Alternatively, the intermediate portion may define a non-uniform radius of curvature along the central curved axis L1. In a preferred embodiment, the curvature of the intermediate portion may be smooth and continuous. Alternatively, the curvature of the intermediate portion may be defined by a series of substantially straight sections (not shown), with each substantially straight section aligned along an individual longitudinal axis corresponding to the individual section, where the magnitude of an angle α with respect to a perpendicular reference axis extended from the proximal end 102 a increases in magnitude with the distance of each subsequent straight section from the proximal end 102 a.

The arcuate fixation member 12C may have a head 106 defined at the proximal end 102 a of the body 102. The head 106 may extend radially outward from the proximal end 102 a of the body 102 in a direction perpendicular to the longitudinal axis L1. In an example embodiment, the head 106 may extend from the body 102 in a direction generally opposite from the direction of curvature of the body 102, as depicted in FIGS. 1A-B. In alternative embodiments, the head 106 may extend from the body 102 in a direction generally towards the direction of curvature of the body 102. The head may define an upper surface 106 a configured for multi-angular engagement with a complementary surface of a delivery instrument, and a lower surface 106 b opposite the upper surface 106 a and configured to engage another component of the intervertebral implant system 100, for example the insert plate 116, when the arcuate fixation member 12C is in a fully inserted position.

Referring now to FIGS. 2A-C, the intervertebral implant spacer, or spacer 108 is defined by a posterior side 108 a, an anterior side 108 b opposite the posterior side, lateral sides 108 c, an upper surface 108 d, and a lower surface 108 e opposite the upper surface. In an example embodiment, a portion of the posterior side 108 a between the lateral sides 108 c may be curved inwardly in the direction of the anterior side 108 b, defining a rounded, generally rectangular kidney-like footprint, as depicted in FIG. 2A. In an alternative embodiment, a portion of the posterior side 108 a between the lateral sides 108 c may be curved outwardly in a direction away from the anterior side 108 b (not shown). In another alternative embodiment, the posterior side 108 a may be substantially straight between the lateral sides 108 c, defining a rounded, generally rectangular footprint (not shown). The spacer 108 may have a central bore 110 defined therethrough, the shape of which substantially conforms to the footprint of the spacer 108 (e.g., a rounded, generally rectangular kidney-like footprint, or a rounded, generally rectangular footprint, depending upon the geometry of the posterior side 108 a). The central bore 110 can be filled with bone growth inducing substances to allow bony ingrowth and to assist in fusion between the spacer 108 and adjacent vertebral bodies.

In an example embodiment of the spacer 108, the upper and lower surfaces 108 d and 108 e may have gripping structures 108 h such as teeth, spikes, or similar structures, defined thereon and configured to facilitate gripping engagement between the upper and lower surfaces 108 d and 108 e and the end plates of adjacent vertebral bodies. The teeth 112 may be pyramidal, saw toothed or other similar shapes. In alternative embodiments of the spacer 108, portions of and/or the entirety of the upper and lower surfaces 108 d and 108 e may be substantially smooth and devoid of any protrusions. Upper and lower edges 108 f and 108 g, defined where the upper and lower surfaces 108 d and 108 e intersect with the posterior, anterior, and lateral sides 108 a, 108 b, and 108 c respectively around the outer perimeter of the spacer 108, may be rounded (not shown). In an example embodiment, the upper and lower edges 108 f and 108 g may be rounded using a uniform radius of curvature around the perimeter of the implant. In an alternative embodiment, the upper and lower edges 108 f and 108 g may be rounded using a non-uniform radius of curvature around the perimeter of the implant. In another alternative embodiment, the upper and lower edges 108 f and 108 g along the anterior side 108 b may be rounded with a greater radius than the remainder of the upper and lower edges 108 f and 108 g, such that a bull nose outer surface (not shown) is created on the anterior side 108 b of the implant. Rounding upper and lower edges 108 f and 108 g may facilitate easier insertion of the spacer 108, for example by minimizing required distraction of the end plates of adjacent vertebral bodies.

In an example embodiment, the spacer 108 has a generally wedge-shaped side-view profile. As illustrated in FIG. 2C, this wedge shape is defined by a gradual decrease in the height of the spacer 108 (as measured between the upper and lower surfaces 108 d and 108 e) extending between the posterior side 108 a in the direction of the anterior side 108 b. The spacer 108 has a generally constant height between lateral sides 108 c. In alternative embodiments, the spacer 108 may have a gradual increase in height followed by a gradual decrease in height extending from one lateral side 108 c to the other, and/or may have a generally constant height between the posterior and anterior sides 108 a and 108 b, or may have convex and/or concave upper and lower surfaces 108 d and 108 e, thereby defining a gradual increase in height followed by a gradual decrease in height extending from the posterior side 108 a to the anterior side 108 b and from one lateral side 108 c to the other.

A plurality of grooves 112 may be defined on the spacer 108 where the upper and lower surfaces 108 d and 108 e intersect with the anterior side 108 b. The grooves 112 may be concave and may be configured to align with arcuate grooves 128 of the insert plate 116 when the spacer 108 and the insert plate 116 are in an assembled configuration. In an example embodiment, the grooves 112 may be substantially smooth and devoid of any protrusions. Retaining grooves 114 may be defined within the lateral sides 108 c of the spacer 108 between the upper and lower surfaces 108 d and 108 e. The retaining grooves 114 may be configured to releasably engage complementary engaging ribs 120 of the insert plate 116.

Referring now to FIGS. 3A-B, the fixation plate, or insert plate, or insert 116 is defined by a generally C-shaped, channel-like body 118 that includes an anterior side 118 a with upper and lower sides 118 b and 118 c opposite each other, and lateral sides 118 d extending from opposite sides of the anterior side 118 a in a generally perpendicular direction from the anterior side 118 a. The anterior, upper, lower, and lateral sides 118 a, 118 b, 118 c, and 118 d may form a generally channel-like structure (in essence, a cradle) which may be configured to receive the anterior side 108 b and at least a portion of the lateral sides 108 c in partial nested engagement. As such, the upper and lower sides 108 b and 108 c may define gradual increases and/or decreases in height in a posterior direction from the anterior side 118 a and/or between the lateral sides 108 d, in order to generally conform the insert plate 116 to the geometry of the spacer 108. The lateral sides 118 d may have engaging ribs 120 defined thereon at the ends opposite the anterior side 118 a, the engaging ribs 120 configured to be releasably received within the retaining grooves 114 of the spacer 108.

The anterior side 118 a of the insert plate 116 may have a pair of apertures 122 defined therethrough configured to receive grasping members of a delivery instrument. In an example embodiment, the apertures 122 may be D-shaped, as illustrated in FIG. 3A. However any other aperture shape may be defined as appropriate. The apertures 122 may have a retaining rib 124 defined therein configured to engage with a complementary grasping rib of the delivery instrument. The anterior side 118 a of the insert plate 116 may also have a central bore 126 defined therethrough having an inner surface 126 a with threads configured to engage complementary threads of a locking screw 138. The anterior side 118 a of the insert plate 116 may also have a concave recess 130 defined therein configured to receive a complementary convex surface 134 d of the blocking plate 132.

The anterior side 118 a of the insert plate 116 may also have a plurality of arcuate grooves 128 defined therethrough configured to slidably receive the arcuate fixation members 12C and to define an insertion trajectory for each of the arcuate fixation members 12C. In an example embodiment, the arcuate grooves 128 may have a generally uniform cross sectional geometry configured to closely conform to the cross sectional geometry of the body 102 of the arcuate fixation member 12C between the head 106 and the distal end 102 b. When an arcuate fixation member 12C is in a fully inserted position within a respective arcuate groove 128, the lower surface 106 b of the head 106 will be engaged with the outer surface of the anterior side 118 a of the insert plate 116. Because the upper surface 106 a of the head 106 will not be flush with the outer surface of the anterior side 118 a of the insert plate 116 in this configuration, it may be desirable to omit the blocking plate 132 and the locking screw 138. In an alternative embodiment, the arcuate grooves 128 have a recessed ledge defined therein in the area where the arcuate grooves 128 intersect with the outer surface of the anterior side 118 a of the insert plate 116, the recessed ledge being configured to receive the lower surface 106 b of the head 106 when the arcuate fixation member 12C is in a fully inserted position, such that the upper surface 106 a of the head 106 is substantially flush with the outer surface of the anterior side 118 a of the insert plate 116.

The arcuate grooves 128 may be disposed about the central bore 126 in any desired configuration and may define any insertion trajectories as appropriate. In the example embodiment depicted in FIGS. 3A-B, the arcuate grooves 128 are defined in opposing quadrants around the central bore 126, with two arcuate grooves 128 located near the upper side 118 b and defining two generally cranial insertion trajectories, and two arcuate grooves 128 located near the lower side 118 c and defining two generally caudal insertion trajectories. It should be noted that this configuration of arcuate groove 128 locations and arcuate fixation member 12C insertion trajectories is merely an example, and the scope of the instant disclosure should not be limited thereto.

Referring now to FIGS. 4A-B, the blocking plate 132 is defined by a generally disc-shaped body 134 with upper and lower surfaces 134 a and 134 b that can be planar as illustrated, an anterior surface 134 c, and a posterior surface 134 d. The disc-shaped body 134 can further define opposed side surfaces 135 a and 135 b, which can be convexly curved, extending between the upper and lower surfaces 134 a-b. The upper and lower surfaces 134 a and 134 b and the height of the body 134 (as measured between the upper and lower surfaces 134 a and 134 b) may be defined to match the height (as measured between the upper and lower surfaces 118 b and 118 c) of the anterior side 118 a of the insert plate 116 when the blocking plate 132 is in a fully assembled configuration. The anterior surface 134 c of the body 134 may be generally planar, or may be defined to match the outer surface of the anterior side 118 a of the insert plate 116 when the blocking plate 132 is in a fully assembled configuration. The posterior surface 134 d may be defined as a convex surface configured to engage with the concave recess 130 of the insert plate 116 when the blocking plate 132 is in a fully assembled configuration.

The posterior surface 134 d can also be configured to engage the heads 106 of the arcuate fixation members 12C inserted into the arcuate grooves 128 of the insert plate 116. For example, the posterior surface 134 d can operate to drive the arcuate fixation members 12C into a fully inserted position within the insert plate 116 as the locking screw 138 is tightened. In addition to driving the arcuate fixation members 12C into a fully inserted position, the blocking plate 138 can additionally prevent backout of the arcuate fixation members 12C. It should be appreciated that the posterior surface 134 d of the blocking plate 132 is not limited to the illustrated convex surface, and that the posterior surface 134 d can define alternative geometries. For example, the posterior surface 134 d may define a plurality of angled surfaces, such as four angled surfaces in opposed quadrants of the posterior surface 134 d, each of the angled surfaces configured to engage with the head 106 of a corresponding arcuate fixation member 12C.

The body 134 may have an aperture 136 defined therethrough. In an example embodiment, the diameter of the aperture 136 may be slightly larger than the diameter of the central bore 126 of the insert plate 116, such that a locking screw 138 may be inserted into the aperture 136 with no interference therebetween. In another embodiment, the diameter of the aperture 136 may be substantially the same as that of the central bore 126, and the inner surface of the aperture 136 may have threads defined thereon, the threads configured to engage complementary threads of the locking screw 138. The aperture 136 may further be defined by a concave recess 136 a defined within the anterior surface 134 c, the concave recess 136 a configured to receive the convex head 142 of the locking screw 138.

It should be appreciated that the blocking plate 132 can be geometrically configured as desired so as to be received and nest in the concave recess 362 and coupled to the insert plate 350. For instance, referring to FIG. 4C, the upper and lower surfaces 134 a-b of the disc-shaped body 134 can be curved, and bow outwards in accordance with one embodiment. Furthermore, the side surfaces 135 a-b can extend substantially straight between the upper and lower surfaces 134 a-b. The disc-shaped body 134 can further define beveled surfaces 137 a-d that are connected between respective side surfaces 135 a and 135 b and respective upper and lower surfaces 134 a and 134 b. Pockets 139 a-b can be defined extending into the side surfaces 135 a-b, the pockets 139 a-b configured to receive a driving instrument that braces against the blocking plate 132 so as to drive the locking screw 138 into the insert plate 350.

Referring now to FIG. 5, the locking screw 138 includes a shaft 140 that defines longitudinally opposing proximal and distal ends 140 a and 140 b, respectively, and a head 142 coupled to the proximal end 140 a of the shaft 140, either directly or indirectly via an unthreaded neck 144 that is coupled between the proximal end 140 a of the shaft 140 and the head 142. The head 142 can define a generally convex shape between the interface of the head 142 and the neck 144 that extends outward towards a proximal end 142 a of the head 142. The convex shape of the head may be configured to engage the concave recess 136 a of the blocking plate 132. Of course, the head 142 can assume any other suitable alternative shape as appropriate. Helical threads 146 extend radially out from the shaft 140 at locations at and between the proximal and distal ends 140 a and 140 b that are configured to engage complementary threads on the inner surface 126 a of the central bore 126 of the insert plate 116. Thus, a substantial entirety of the shaft 140 between the proximal and distal ends 140 a and 140 b may be threaded. The distal end 142 a of the head 142 may have driving members 142 b defined therein, designed to engage with complementary driving members of a delivery instrument. It should be appreciated that the locking screw 138 can alternatively be provided in combination with the blocking plate 132 as a captive locking screw, wherein the locking screw 138 is rotatably retained within the aperture 136 of the blocking plate 132. It should be appreciated that the head 142 can be externally threaded.

Referring now to FIGS. 6A-C, an example embodiment of the intervertebral implant system 100 is illustrated in an exploded view and in a nearly completely assembled configuration. FIG. 6B depicts the intervertebral implant system 100 partially assembled outside of an intervertebral space (the blocking plate 132 and locking screw 138 have been omitted for simplicity). The spacer 108 has been seated within the insert plate 116 such that the retaining ribs are seated with the retaining grooves 114 on the lateral sides of the spacer 108. Four arcuate fixation members 12C have been inserted through corresponding arcuate grooves 128 within the insert plate 116, and have been driven to an almost fully inserted position. In a final assembled configuration, the arcuate fixation members 12C would be driven into their fully inserted position, the blocking plate 132 would be received within the concave recess 130 in the anterior side of the insert plate 116, and the locking screw 138 would be driven into the central bore 126 of the insert plate 116 and finally tightened, thereby blocking the arcuate fixation members 12C from backing out of the assembled intervertebral implant system 100.

FIG. 6C depicts an example embodiment of the intervertebral implant system 100 partially assembled inside of an intervertebral space between adjacent vertebral bodies V6 and V7 (the blocking plate and locking screw have been omitted for simplicity). As an initial step, the spacer 108 has been prepared for insertion, for example by being packed a with bone growth inducing substance and or/having its outer surfaces properly prepared, and has been seated within the insert plate 116 such the retaining ribs are seated with the retaining grooves on the lateral sides of the spacer 108. The spacer 108 was then inserted into the intervertebral space between the adjacent vertebral bodies V6 and V7 using a delivery instrument (not shown). The delivery instrument was then used to deliver the four arcuate fixation members 12C into the arcuate grooves in the fixation plate 116 and drive them into an almost fully inserted position. During the final steps of the assembly process, the delivery instrument would be used to drive the arcuate fixation members 12C into their fully inserted position, the blocking plate would be received within the concave recess in the anterior side of the insert plate 116, and the locking screw would be driven into the central bore of the insert plate 116 and finally tightened, thereby blocking the arcuate fixation members 12C from backing out of the assembled intervertebral implant system 100.

Now referring generally to FIGS. 7A-14B, alternative example embodiments of components of the intervertebral implant system 100, for instance arcuate fixation member 12D, intervertebral implant spacers 316 and 336, and insert plate 350, are illustrated. Various embodiments of an intervertebral implant 400 can be constructed from the components of the intervertebral implant system 100, as described in more detail below. It should be noted preliminarily that in the interest of brevity, the figures and subsequent description pertaining to the arcuate fixation member 12D do not refer to certain features and/or uses of the arcuate fixation member 12C that may be integrated into the arcuate fixation member 12D, for example the use of the arcuate fixation member 12C in combination with above-described components of the intervertebral implant system 100, for instance the intervertebral implant spacer 108, the insert plate 116, the blocking plate 132, or the locking screw 138. However, embodiments in which those and other features of the arcuate fixation member 12C are integrated into the arcuate fixation member 12D are intended to be within the scope of the instant disclosure.

Referring now to FIGS. 7A-J, an alternative embodiment of the arcuate fixation member is illustrated. The arcuate fixation member 12D includes a fixation body, or body 300 defining a proximal end 300 a, a distal end 300 b opposite the proximal end, and an intermediate portion 300 c extending between the proximal and distal ends 300 a-b, respectively. The fixation body 300 has a cross sectional geometry that is substantially hexagonal, defining opposing laterally convex front and rear surfaces 300 e-f extending between opposing sides, or edges 300 d. The fixation body 300 defines a cross sectional geometry that is substantially constant throughout the intermediate portion 300 c of the fixation body 300, and is tapered between lateral surfaces 301 converging along the edges 300 d near the distal end 300 b, defining a tip 302 configured to cut into an underlying structure, such as bone. The intermediate portion 300 c of the fixation body 300 is curved along a central curved axis L1. It should be appreciated that the central curved axis L1 can define an insertion trajectory of the arcuate fixation member 12D into underlying structure, such as a vertebral body. It should be appreciated that the insertion trajectory can be differently defined, for example in accordance with alternative geometries of the arcuate fixation member 12D. In an embodiment, the intermediate portion 300 c is curved along substantially the entire length of the fixation body 300 between the proximal and distal ends 300 a-b, respectively. Alternatively, one or more distinct portions of the intermediate portion 300 c can be curved (not shown).

In the illustrated embodiment, the intermediate portion 300 c is curved along the central curved axis L1 in accordance with a uniform radius of curvature R1. Alternatively, the intermediate portion 300 c can define a non-uniform radius of curvature along the central curved axis L1. In a preferred embodiment, the curvature of the intermediate portion 300 c may be smooth and continuous. Alternatively, the curvature of the intermediate portion 300 c can be defined by a series of substantially straight sections (not shown), with each substantially straight section aligned along an individual longitudinal axis corresponding to the respective individual section, where the magnitude of an angle α with respect to a perpendicular reference axis A extended from the proximal end 300 a increases in magnitude with the distance of each subsequent straight section from the proximal end 300 a. It should be appreciated that the cross sectional geometry of the fixation body 300 is not limited to the illustrated substantially hexagonal shape, and that the fixation body 300 can alternatively be defined with any suitable cross sectional geometry. It should further be appreciated that the cross sectional dimension of the fixation body 300 may vary, for example increasing or decreasing, throughout one or more portions of the intermediate portion 300 c.

The arcuate fixation member 12D may have a head 304 defined at the proximal end 300 a of the fixation body 300. The head 304 may extend radially outward from the proximal end 300 a of the fixation body 300 in a direction perpendicular to the central curved axis L1. In an example embodiment, the head 304 may extend from the fixation body 300 in a direction generally towards the direction of curvature of the fixation body 300, as depicted in FIGS. 7A-D. In alternative embodiments, the head 304 may extend from the fixation body 300 in a direction generally opposite from the direction of curvature of the fixation body 300. The head 304 may define an upper surface 304 a configured for multi-angular engagement with a complementary surface of a delivery instrument, and a lower surface 304 b opposite the upper surface 304 a and configured to engage another component of the intervertebral implant system 100, for example the insert plate 350, when the arcuate fixation member 12D is in an inserted position. The head 304 can have one or more tapered surfaces, for instance surface 304 c, defined thereon, the tapered surface 304 c configured to engage with a complementary surface in another component of the intervertebral implant system 100, for example the insert plate 350, thereby locking the arcuate fixation member 12D in an inserted position.

The fixation body 300 can define one or more guidance members, the guidance members configured to guide the tip 302 along an insertion trajectory as the arcuate fixation member 12D is inserted into an underlying structure, such as a vertebral body. In the illustrated embodiments, guidance members are disposed at distal end 300 b of the fixation body 300, and in particular near the tip 302, but can alternatively be defined at any location on the fixation body 300. The fixation body 300 can define guidance members that are recessed within the fixation body 300, such as the illustrated flutes 306, or guidance members that comprise projections extending from the fixation body 300, such as the illustrated outer wings 303 and/or the keel 308, in any combination. For example, in the illustrated embodiment, a pair of recessed guidance flutes, or flutes 306 are defined by a keel 308 disposed between opposing wings 303.

The illustrated flutes 306 are defined by and are disposed at the tip 302 of the fixation body 300, the flutes 306 extending into the fixation body 300 from the tip 302 along directions substantially parallel to each other and to the insertion trajectory of the arcuate fixation member 12D, and terminating in the intermediate section 300 c of the fixation body 300 proximal from the tip 302. In alternative embodiments, the flutes 306 can extend along directions that are angularly offset or otherwise non-parallel with respect to each other and/or with respect to the insertion trajectory. The flutes 306 are not limited to the illustrated length, and can alternatively be defined to terminate within the tip 302 of the fixation body, or to extend along any length, up to the entirety, of the fixation body 300. It should be appreciated that the flutes 306 can be symmetrically with respect to each other as illustrated, or asymmetrically. For example the flutes 306 can be defined with matching or different geometries, equal or different lengths, equal or different depths, etc.

The illustrated flutes 306 have a substantially “V” shaped geometry defined by outer wings, or wings 303 defined in the fixation body 300 and inner surfaces, or keel surfaces 305 defined in the fixation body 300, the wings 303 and keel surfaces 305 converging in troughs 307. The keel surfaces 305 define a keel 308, as described in more detail below, the flutes 306 are disposed between respective wings 303 and the keel 308. It should be appreciated that the wings 303 are not limited to the illustrated offset wings 303 disposed adjacent the keel 308 on respective sides of the keel 308, and that a single, up to a plurality of wings 303 can be defined at any location in the fixation body 300, for example substantially centrally between the edges 300 d, offset laterally toward either edge 300 d, or substantially along either edge 300 d. It should further be appreciated that the wings 303 and/or the keel surfaces 305 are not limited to being defined within the cross sectional geometry of the fixation body 300, and can alternatively be defined to extend outwardly from the fixation body 300, for example from the front or rear surfaces 300 e-f and/or the edges 300 d. It should further still be appreciated that the geometries of the flutes 306 are not limited to the illustrated “V” shape, and can alternatively be defined with any suitable geometry.

The keel surfaces 305 define a projection from the fixation body 300, the projection configured as a guidance member in the form of a guidance keel, or keel 308. In the illustrated embodiment, the keel 308 is defined substantially centrally between the edges 300 d of the fixation body 300, and disposed between the wings 303. In alternative embodiments, the keel 308 can be laterally offset toward either edge 300 d. It should be appreciated that the arcuate fixation member 12D is not limited to a single keel 308 as illustrated, and that the fixation body 300 can define a plurality of keels 308 at any locations in the fixation body 300. It should further be appreciated that the arcuate fixation member 12D is not limited to the illustrated configuration of guidance members, and that the fixation body 300 can be differently constructed with any number of wings 303, flutes 306, keels 308, or any other guidance members, in any combination.

The fixation body 300 of the arcuate fixation member 12D can define one or more gripping structures configured to be retain the arcuate fixation member 12D in an inserted position within an underlying structure, such as a vertebral body. The gripping structures can include protrusions defined on the fixation body 300, such as teeth, spikes, or similar structures. For example, in the illustrated embodiment, a plurality of teeth 310 are defined in rows on opposing sides of the fixation body 300, in particular in the intermediate portion 300 c of the fixation body 300 along the edges 300 d. The illustrated plurality of teeth 310 are defined by a corresponding plurality of substantially “V” shaped notches 312 defined along the edges 300 d of the fixation body 300. In the illustrated embodiment, the notches 312 are defined in parallel directions with respect to each other, such that the magnitude of an angle β between each notch 312 and the perpendicular reference axis A is maintained. In alternative embodiments, the notches 312 can be defined in directions that are not parallel with respect to each other, for example such that the magnitude of the angle β increases with the distance of each successive notch 312 from the proximal end 300 a of the fixation body 300.

It should be appreciated that the gripping structures are not limited to being defined along the edges 300 d of the fixation body 300, and that gripping structures supplemental to, or in lieu of, the illustrated teeth 310 can alternatively be defined in any other suitable location on the fixation body 300. It should further be appreciated that the gripping structures are not limited to the gripping structure geometry of the illustrated teeth 310, and that the fixation body 300 can alternatively define any other suitable gripping structure geometry. It should further still be appreciated that the number and/or geometry of the gripping structures can be defined so to add bone growth surface area to the arcuate fixation member 12D.

One or more removal members can be defined in the fixation body 300 of the arcuate fixation member 12D, the removal members allowing for distraction of the arcuate fixation member 12D from an underlying structure, such as a vertebral body. For example, in the embodiment illustrated in FIGS. 7A-H, a pair of grooves 314 are defined at the proximal end 300 a of the fixation body 300, the grooves 314 extending into the fixation body 300 from the edges 300 d. The illustrated grooves 314 are sized to receive complementary members of a removal tool. In an alternative embodiment illustrated in FIGS. 7I-J, a single groove 314 is defined at the proximal end 300 a of the fixation body 300, the groove 314 extending into the rear surface 300 f. It should be appreciated that the arcuate fixation member 12D is not limited to the illustrated removal members, and that the fixation body 300 can be alternatively be defined with one or more other suitable removal members.

Referring now to FIGS. 8A-D, an alternative embodiment of the intervertebral implant spacer, or spacer is illustrated. The intervertebral implant spacer, or spacer 316 defines a spacer body, or body 318 configured to be implanted into an intervertebral space, the spacer body 318 having an outer wall 318 c that defines an enclosed perimeter of the spacer body 318. In the illustrated embodiment, the outer wall 318 c comprises an anterior wall 318 a extending between opposing ends 318 b, a posterior wall 318 d opposite the anterior wall 318 a, and opposing side walls 318 e, the side walls 318 e extending between the ends 318 b of the anterior wall 318 a and the posterior wall 318 d. The spacer body 318 defines an upper surface 318 f, and a lower surface 318 g opposite the upper surface. The outer wall 318 c defines an aperture 322 extending into the spacer body 318 through at least one of the upper or lower surfaces 318 f-g.

A portion, up to an entirety of the anterior wall 318 a can be curved inwardly toward the posterior wall 318 d, defining an apex of curvature, or apex 320 in the anterior wall 318 a approximately midway between the opposing ends 318 b, as depicted in FIGS. 8A-B. Of course the apex 320 can be defined at any other location along the anterior wall 318 a. In alternative embodiments, the anterior wall 318 a can be straight between the ends 318 b, can be curved outwardly away from the posterior wall 318 d, or can define one or more distinct straight portions and/or curved portions between the ends 318 b, thereby defining a corresponding number of apices 320 along the anterior wall 318 a. It should be appreciated that the shape of the perimeter of the spacer body 318 is not limited to the illustrated geometry, and that the outer wall 318 c can be differently constructed to define an alternatively shaped perimeter geometry of the spacer body 318.

The spacer body 318 can further include an inner wall 318 h, the inner wall 318 h defined so as to divide the aperture 322 defined by the outer wall 318 c into a plurality of apertures 322. For example, in the illustrated embodiment, the inner wall 318 h divides the aperture 322 defined by the outer wall 318 c into a pair of apertures 322. The illustrated inner wall 318 h extends between the apex 320 of the anterior wall 318 a and the outer wall 318 c, in particular between the apex 320 and substantially the midpoint of the posterior wall 318 d. At least one additional aperture 322 can be defined between the anterior wall 318 a and an insert plate, such as insert plate 350 (See FIGS. 10A-F) when the insert plate 350 is coupled to the spacer 316. One or more of the plurality of apertures 322 can be filled with bone growth inducing substances, for example to allow bony growth ingress and/or egress with respect to the spacer 316 and to assist in fusion between the spacer 316 and adjacent vertebral bodies.

In alternative embodiments, the spacer body 318 can be differently constructed, thereby alternatively defining the plurality of apertures 322. For example, it should be appreciated that the inner wall 318 h can alternatively be defined to extend between any respective locations on the anterior wall 318 a and the outer wall 318 c. It should further be appreciated that the spacer body 318 is not limited to a single inner wall 318 h as illustrated, and that alternatively a plurality of inner walls 318 h having any combination of straight or curved geometries can be defined, the inner walls 318 h of the plurality of inner walls 318 h extending between a single or multiple locations on the anterior wall 318 a and a single or multiple corresponding locations on the outer wall 318 c, extending between respective locations on one or more inner walls 318 h and the outer wall 318 c, extending between a single or multiple locations on the outer wall 318 c, extending from a single or multiple locations on the anterior wall 318 a in a generally outward direction away from the posterior wall 318 d, or any combination thereof. It should further still be appreciated that the respective thicknesses of the anterior wall 318 a, the outer wall 318 c, and/or the inner wall 318 h can be uniform, or can have one or more portions of varying thickness.

One or more portions, up to an entirety of surfaces of the spacer body 318, for instance interior surfaces such as the inner surfaces 318 c′ of the outer wall 318 c and/or the inner surfaces 318 h′ of the inner wall 318 h, can be configured to allow bony ingrowth into the respective surfaces by bone growth inducing substances disposed into the apertures 322, for instance to enhance fusion between the spacer 316 and adjacent vertebral bodies and/or to provide a form of secondary fixation between an intervertebral implant 400 constructed with the spacer 316 and adjacent vertebral bodies. For example, one or more portions of the inner surface 318 c′ of the outer wall 318 c can be recessed, defining respective cavities 324 therein. The cavities 324 can be open to respective apertures 322, such that the cavities 324 can be filled with bone growth inducing substances and/or to allow the above-described bony ingrowth into the cavities 324. It should be appreciated that the spacer body 318 is not limited to the illustrated cavities 324, and that the surfaces of the spacer body 318 can be differently constructed with any other geometries in order to allow body ingrowth.

The apertures 322 defined in the spacer body 318 can be configured to be in communication with each other, for example to facilitate biological communication between bone growth inducing substances in respective apertures 322 and/or to allow bony growth ingress and/or egress between the apertures 322. For example, one or more openings, such as openings 326 can be defined through the outer wall 318 c and/or the inner wall 318 h, the openings 326 placing two or more of the plurality of apertures 322 in communication with each other. In the illustrated embodiment, a pair of openings 326 are defined through the outer wall 318 c, and in particular the anterior wall 318 a. It should be appreciated that the spacer body 318 can alternatively configured to define one, up to a plurality of openings 326 through the outer wall 318 c and/or the inner wall 318 h at any locations along the outer wall 318 c and/or the inner wall 318 h.

The spacer 316 is configured to be coupled to an insert plate, such as insert plate 350. Coupling members can be defined on the spacer body 318, the coupling members configured to releasably mate with complementary coupling members of an insert plate. For example, in the illustrated embodiment, coupling members in the form of retaining grooves 328 are defined in the ends 318 b of the anterior wall 318 a, the retaining grooves 328 extending into the spacer body 318 from open ends 328 a defined in the lower surface 318 g and terminating in closed ends 328 b near the upper surface 318 f. The retaining grooves 328 are configured to receive complementary retaining members, such as the retaining members 356 defined on the insert plate 350, therein. The closed ends 328 b of the retaining grooves 328 can operate to retain the retaining members 356 of an insert plate within the retaining grooves 328 and/or act as stops to ensure proper alignment between an insert plate and the spacer 316 during assembly. In an alternative embodiment, the spacer 316 can be constructed such that the retaining grooves 328 extend along the entirety of the body 318, such that both ends 328 a-b are open.

Interlocking members can be defined on the coupling members, the interlocking members configured to be received in releasably locking engagement with complementary interlocking members defined on the retaining members 356 of the insert plate 350. For example, in the illustrated embodiment, interlocking members in the form of locking ridges 330 are defined in the retaining grooves 328, the locking ridges 330 sized to be received in releasably locking engagement within complementary locking grooves 358 defined on the retaining members 356 of the insert plate 350. In addition to locking the insert plate 350 into position with respect to the spacer 316, the interlocking members can be configured to facilitate a desired alignment in the transverse, or cranial-caudal direction between the insert plate and the spacer 316. For example, the illustrated locking ridges 330 are located within the retaining grooves 328 at a location approximately equal to the height wise midpoint of the anterior wall 318 a, thereby ensuring that when the retaining members 356 are inserted into the retaining grooves 328 such that the locking ridges 330 are received in the locking grooves 358 (see FIG. 11B), the spacer 316 and the insert plate will achieve a desired transverse alignment with respect to each other.

The upper and lower surfaces 318 f-g of the spacer body 318 can define a plurality of relief members, such as relief grooves 332, the relief grooves 332 configured to align with guide apertures 366 of the insert plate 350 (see FIGS. 10A-E) and to partially receive the fixation bodies 300 of respective arcuate fixation members 12D therein when an intervertebral implant 400 is assembled from the spacer 316 and an insert plate 350 and one or more arcuate fixation members 12D are inserted into the guide apertures 366 of the insert plate 350 and driven into position in an underlying structure, such as a vertebral body. In the illustrated embodiment, the relief grooves 332 are concave and are substantially smooth and devoid of any protrusions. It should be appreciated that the spacer 316 can be alternatively constructed without the relief grooves 332.

The upper and lower surfaces 318 f-g of the spacer body 318 can be configured as bone-engaging surfaces, for example by defining gripping structures thereon, such as teeth, spikes, or the like. The gripping structures can be configured to engage adjacent underlying structures, such as the endplates of adjacent vertebral bodies, when the intervertebral implant 400 is inserted into an intervertebral space. In the illustrated embodiment, the upper and lower surfaces 318 f-g have teeth 334 defined thereon. The teeth 334 may be pyramidal, saw toothed or other similar shapes. In alternative embodiments of the spacer 316, portions of, up to the entirety of the upper and/or lower surfaces 318 f-g can be substantially smooth and devoid of any gripping structures.

The upper perimeter edge, or upper edge 318 f′ and the lower perimeter edge, or lower edge 318 g′ of the spacer body 318, defined along the outer periphery of the spacer body 318 where the outer surface of the outer wall 318 c intersects with the upper and lower surfaces 318 f-g, respectively, can be rounded. Rounding the upper and lower edges 318 f′-g′ can facilitate easier insertion and/or removal of the spacer 316, and thus the intervertebral implant 400, from an intervertebral space, for example by minimizing required distraction of the end plates of adjacent vertebral bodies. Distinct portions, up to an entirety of the upper and lower edges 318 f′-g′ can be rounded using a varying radius of curvature. For example, in the illustrated embodiment respective portions of the upper and lower edges 318 f′-g′ along the posterior wall 318 d are rounded with a greater radius of curvature than the remainder of the upper and lower edges 318 f′-g′, such that a “bullet tip” profile is defined on the posterior wall 318 d of the spacer body 318, as depicted in FIG. 8D. In alternative embodiments, the upper and lower edges 318 f′-g′ can be rounded using a substantially constant radius of curvature.

The upper and lower surfaces 318 f-g can be defined as partially, up to fully convex surfaces. In the illustrated embodiment, the convexity of the upper and lower surfaces 318 f-g in the anterior-posterior direction between the anterior wall 318 a and the posterior wall 318 d differs from the convexity of the upper and lower surfaces 318 f-g in the lateral direction between the side walls 318 e. The upper and lower surfaces 318 f-g are fully convex in the anterior-posterior direction, and exhibit asymmetric convexity with respect to each other, wherein the anterior-posterior convexity of the upper surface 318 f is defined using a shorter radius than the radius used to define the convexity of the lower surface 318 g. In other words, the upper surface 318 f exhibits a greater amount of curvature than the lower surface 318 g. The upper and lower surfaces 318 f-g are partially convex in the lateral direction, and exhibit symmetric convexity with respect to each other, wherein the lateral convexities of the upper and lower surfaces 318 f-g are equal, or mirror images of each other. In particular, the upper and lower surfaces 318 f-g define substantially no convexity in the lateral direction throughout the region C2, and are convex in the lateral direction in the regions C1 near the side walls 318 e.

It should be appreciated that the geometry of the upper and lower surfaces 318 f-g is not limited to the convexity of the illustrated embodiment, and that the upper and lower surfaces 318 f-g can be defined with full or partial convexity in the anterior-posterior and/or lateral directions, with full or partial concavity in the anterior-posterior and/or lateral directions, with a combination of partial convexity and concavity in the anterior-posterior and/or lateral directions, or with no curvature at all (i.e., substantially flat) in the anterior-posterior and/or lateral directions. It should further be appreciated that the regions C1 and C2 can be defined with wider or narrower widths in the lateral direction. It should further still be appreciated that the geometry of the upper and lower surfaces 318 f-g can be defined either symmetrically or asymmetrically with respect to each other.

Referring now to FIGS. 8C-D, the illustrated embodiment of the spacer 316 has a generally wedge shaped side view profile defined by a gradual increase in height followed by a gradual decrease in height between the anterior wall 318 a and the posterior wall 318 d, and a generally rectangular front view profile defined by a generally constant height throughout the C2 region, and gradually decreasing height throughout the C1 regions between the opposing ends of the C2 region and the side walls 318 e. In alternative embodiments the height between the anterior wall 318 a and the posterior wall 318 d of the spacer 316 may gradually decrease, may gradually increase, may have a gradual decrease followed by a gradual increase, or may be generally constant, while the height between the side walls 318 e may increase and/or decrease, or may be generally constant.

The geometry of the spacer 316, for instance the geometry of the upper and lower surfaces 318 f-g and/or the difference in the height of the body 318 between the anterior and posterior walls 318 a, 318 d defines a lordotic angle θ of the spacer 316. The lordotic angle θ defined by the spacer 316 can be increased and/or decreased by varying the geometry of the spacer 316. For example, the lordotic angle θ defined by the illustrated spacer 316 can be increased by heightening the anterior wall 318 a of the spacer 316 while maintaining the height of the posterior wall 318 d. In preferred embodiments, the anterior-posterior convexity defined by the upper surface 318 f is increased with increasing magnitude of the lordotic angle θ, while the anterior-posterior convexity defined by the lower surface 318 g is maintained. It should be appreciated that when the geometry of the spacer 316 is alternatively constructed in order to increase or decrease the lordotic angle θ defined by the spacer 316, the anterior-posterior convexity and/or the lateral convexity of the upper and/or lower surfaces 318 f-g can be increased or decreased in any combination such that the upper and lower surfaces 318 f-g are defined the same or differently.

Referring now to FIGS. 9A-D, another alternative embodiment of the intervertebral implant spacer, or spacer is illustrated. The intervertebral implant spacer, or spacer 336 defines a generally hollow spacer body, or body 338 having an open anterior end 338 a defined between opposing ends 338 b, an outer wall 338 c extending around a perimeter of the spacer body 336 between the ends 338 b, and opposing upper and lower plates 338 f-g, the outer wall 338 c extending between the upper and lower plates 338 f-g. The upper and lower plates 338 f-g define respective upper and lower surfaces 338 h-i. In the illustrated embodiment, the outer wall 338 c is defined by a posterior wall 338 d opposite the anterior end 338 a and opposing side walls 338 e, the side walls 338 e extending between the ends 338 b and the posterior wall 338 d. It should be appreciated that the shape of the perimeter of the spacer body 338 is not limited to the illustrated geometry, and that the outer wall 338 c can be differently constructed to define an alternatively shaped perimeter geometry of the spacer body 338.

The spacer body 338 can have a plurality of openings, such as apertures 340 and/or slots 342 defined therethrough, for example to allow bony growth ingress and/or egress with respect to the spacer body 338, the bony growth ingress and/or egress assisting in fusion between the spacer 336 and adjacent vertebral bodies and/or providing a form of secondary fixation between an intervertebral implant 400 constructed with the spacer 336 and adjacent vertebral bodies. In the illustrated embodiment, a plurality of apertures 340 are defined extending through the upper and lower plates 338 f-g, and a plurality of slots 342 are defined extending through the outer wall 338 c. The apertures 340 that extend through each of the respective plates can have varying diameters with respect to each other and extend through the plates at locations that define a pattern that can be repeated between the upper and lower plates 338 f-g such that the each of the apertures 340 that extend through the upper plate 338 f are aligned with corresponding apertures that extend through the lower plate 338 g with respect to central axes defined between respective apertures in a substantially transverse direction to the spacer body 338. The slots 342 are equally sized and elongate in the transverse direction between the upper and lower plates 338 f-g, and are spaced equally from each other along the outer wall 338 c.

The generally hollow interior of the spacer body 338 can be filled with bone growth inducing substances, for example to allow bony growth ingress and/or egress with respect to the spacer body 338 as described above. It should be appreciated that spacer body 338 is not limited to the illustrated apertures 340, that the upper and lower plates 338 f-g can alternatively be defined with any number of apertures 340 of varying diameters and/or locations, and that the apertures 340 on the upper and lower plates 338 f-g, respectively, can be defined the same or differently. It should further be appreciated that the spacer body 338 is not limited to the illustrated slots 342, that the outer wall 338 c can alternatively be defined with any number of slots 342 of varying shapes and/or sizes, and that the slots 342 can be spaced apart from each other equally or differently. It should further still be appreciated that the openings defined in the spacer body 338 are not limited to the illustrated apertures 340 and slots 342, and that openings having any other geometry can be defined through the spacer body 338 at any respective locations, in addition to or in lieu of the apertures 340 and slots 342. It should further still be appreciated that the respective thicknesses of the upper plate 338, the lower plate 338 g and/or the outer wall 338 c can be uniform or can have one or more portions of varying thickness.

The spacer 336 is configured to be coupled to an insert plate, such as insert plate 350, such that the open anterior end 338 a is disposed between the posterior end 338 d and the insert plate. Coupling members can be defined on the spacer body 338 of the spacer 336, the coupling members configured to releasably mate with complementary coupling members of an insert plate. For example, in the illustrated embodiment, coupling members in the form of retaining grooves 344 are defined in the ends 338 b of the anterior end 338 a, the retaining grooves 344 extending into the spacer body 338 from open ends 344 a defined in the lower surface 338 i and terminating in closed ends 344 b near the upper surface 338 h. The retaining grooves 344 are configured to receive complementary retaining members, such as the retaining members 356 defined on insert plate 350, therein. The closed ends 344 b of the retaining grooves 344 can operate to retain the retaining members 356 of an insert plate within the retaining grooves 344 and/or act as stops to ensure proper alignment between an insert plate and the spacer 336 during assembly. In an alternative embodiment, the spacer 336 can be constructed such that the retaining grooves 344 extend along the entirety of the body 338, such that both ends 344 a-b are open.

Interlocking members can be defined on the coupling members, the interlocking members configured to be received in releasably locking engagement with complementary interlocking members defined on the retaining members 356 of the insert plate 350. For example, in the illustrated embodiment, interlocking members in the form of locking ridges 346 are defined in the retaining grooves 344, the locking ridges 346 sized to be received in releasably locking engagement within complementary locking grooves 358 defined on the retaining members 356 of the insert plate 350. In addition to locking the insert plate 350 into position with respect to the spacer 336, the interlocking members can be configured to facilitate a desired alignment in the transverse, or cranial-caudal direction between the insert plate and the spacer 336. For example, the illustrated locking ridges 346 are located within the retaining grooves 344 at a location approximately equal to the height wise midpoint of the anterior end 338 a, thereby ensuring that when the retaining members 356 are inserted into the retaining grooves 344 such that the locking ridges 346 are received in the locking grooves 358 (see FIG. 11B), the spacer 336 and the insert plate will achieve a desired transverse alignment with respect to each other.

The upper and lower plates 338 f-g of the spacer body 338 can define a plurality of relief members, such as relief grooves 339, the relief grooves 339 configured to align with guide apertures 366 of the insert plate 350 (see FIGS. 10A-E) and to partially receive the fixation bodies 300 of respective arcuate fixation members 12D therein when an intervertebral implant 400 is assembled from the spacer 336 and an insert plate 350 and one or more arcuate fixation members 12D are inserted into the guide apertures 366 of the insert plate 350 and driven into position in an underlying structure, such as a vertebral body. In the illustrated embodiment, the relief grooves 339 define edges 339 a in the upper and lower surfaces 338 h-i that are substantially smooth and devoid of any protrusions. It should be appreciated that the spacer 336 can be alternatively constructed without the relief grooves 339.

The upper and lower surfaces 338 h-i of the spacer body 338 can be configured as bone-engaging surfaces, for example by defining gripping structures thereon, such as teeth, spikes, or the like. The gripping structures can be configured to engage adjacent underlying structures, such as the endplates of adjacent vertebral bodies, when the intervertebral implant 400 is inserted into an intervertebral space. In the illustrated embodiment, the upper and lower surfaces 338 h-i have teeth 348 defined thereon. The teeth 348 may be pyramidal, saw toothed or other similar shapes. In alternative embodiments of the spacer 336, portions of, up to the entirety of the upper and/or lower surfaces 338 h-i can be substantially smooth and devoid of any gripping structures.

The upper perimeter edge, or upper edge 338 h′ and the lower perimeter edge, or lower edge 338 i′ of the spacer body 338, defined along the outer periphery of the spacer body 338 where the outer surface of the outer wall 338 c intersects with the upper and lower surfaces 338 h-i, respectively, can be rounded. Rounding the upper and lower edges 338 h′-i′ can facilitate easier insertion and/or removal of the spacer 336, and thus the intervertebral implant 400, from an intervertebral space, for example by minimizing required distraction of the end plates of adjacent vertebral bodies. Distinct portions, up to an entirety of the upper and lower edges 338 h′-i′ can be rounded using a varying radius of curvature. For example, in the illustrated embodiment respective portions of the upper and lower edges 338 h′-i′ along the posterior wall 338 d are rounded with a greater radius of curvature than the remainder of the upper and lower edges 338 h′-i′, such that a “bullet tip” profile is defined on the posterior wall 338 d of the spacer body 338, as depicted in FIG. 9D. In alternative embodiments, the upper and lower edges 338 h′-i′ can be rounded using a substantially constant radius of curvature.

The upper and lower surfaces 338 h-i can be defined as partially, up to fully convex surfaces. In the illustrated embodiment, the convexity of the upper and lower surfaces 338 h-i in the anterior-posterior direction between the anterior end 338 a and the posterior wall 338 d differs from the convexity of the upper and lower surfaces 338 h-i in the lateral direction between the side walls 338 e. The upper and lower surfaces 338 h-i are fully convex in the anterior-posterior direction, and exhibit asymmetric convexity with respect to each other, wherein the anterior-posterior convexity of the upper surface 338 h is defined using a shorter radius that the radius used to define the convexity of the lower surface 338 i. In other words, the upper surface 338 h exhibits a greater amount of curvature than the lower surface 338 i. The upper and lower surfaces 338 h-i are partially convex in the lateral direction, and exhibit symmetric convexity with respect to each other, wherein the lateral convexity of the upper and lower surfaces 338 h-i are equal, or mirror images of each other. In particular, the upper and lower surfaces 338 h-i define substantially no convexity in the lateral direction throughout the region C4, and are convex in the lateral direction in the regions C3 near the side walls 338 e.

It should be appreciated that the geometry of the upper and lower surfaces 338 h-i is not limited to the convexity of the illustrated embodiment, and that the upper and lower surfaces 338 h-i can be defined with full or partial convexity in the anterior-posterior and/or lateral directions, with full or partial concavity in the anterior-posterior and/or lateral directions, with a combination of partial convexity and concavity in the anterior-posterior and/or lateral directions, or with no curvature at all (i.e., substantially flat) in the anterior-posterior and/or lateral directions. It should further be appreciated that the regions C3 and C4 can be defined with wider or narrower widths in the lateral direction. It should further still be appreciated that the geometry of the upper and lower surfaces 338 h-i can be defined either symmetrically or asymmetrically with respect to each other.

Referring now to FIGS. 9C-D, the illustrated embodiment of the spacer 336 has a generally wedge shaped side view profile defined by a gradual increase in height followed by a gradual decrease in height between the anterior end 338 a and the posterior wall 338 d, and a generally rectangular front view profile defined by a generally constant height throughout the C4 region, and gradually decreasing height throughout the C3 regions between the opposing ends of the C4 region and the side walls 338 e. In alternative embodiments the height between the anterior end 338 a and the posterior wall 338 d of the spacer 336 may gradually decrease, may gradually increase, may have a gradual decrease followed by a gradual increase, or may be generally constant, while the height between the side walls 338 e may increase and/or decrease, or may be generally constant.

The geometry of the spacer 336, for instance the geometry of the upper and lower surfaces 338 h-i and/or the difference in the height of the body 338 between the anterior end 338 a and the posterior wall 338 d defines a lordotic angle θ of the spacer 336. The lordotic angle θ defined by the spacer 336 can be increased and/or decreased by varying the geometry of the spacer 336. For example, the lordotic angle θ defined by the illustrated spacer 336 can be increased by heightening the anterior end 338 a of the spacer 336 while maintaining the height of the posterior wall 338 d. In preferred embodiments, the anterior-posterior convexity defined by the upper surface 338 h is increased with increasing magnitude of the lordotic angle θ, while the anterior-posterior convexity defined by the lower surface 338 i is maintained. It should be appreciated that when the geometry of the spacer 336 is alternatively constructed in order to increase or decrease the lordotic angle θ defined by the spacer 336, the anterior-posterior convexity and/or the lateral convexity of the upper and/or lower surfaces 338 h-i can be increased or decreased in any combination such that the upper and lower surfaces 338 h-i are defined the same or differently.

Referring now to FIGS. 10A-F, alternative embodiments of the insert plate are illustrated. The insert plate, or insert 350 defines a plate having plate body, or body 352 extending between opposing plate ends 352 a, the plate body 352 defining an anterior side 352 b, a posterior side 352 c opposite the anterior side, an upper surface 352 d, and a lower surface 352 e opposite the upper surface. In the illustrated embodiments, the anterior side 352 b defines a curved outer periphery of the plate body 352. The plate body 352 can define one or more insert members, such as insert slots 354, the insert members configured to receive the complementary members defined on a delivery, or insertion instrument. It should be appreciated that the insert members are not limited to the illustrated insert slots 354, and that the insert members can be alternatively defined in accordance with the complementary insert members of a respective delivery instrument.

The insert plate 350 is configured to be coupled to a spacer, for instance the above-described spacers 316 or 336. Coupling members can be defined on the plate body 352, the coupling members configured to releasably mate with complementary coupling members of a spacer. For example, in the illustrated embodiments, coupling members in the form of retaining members 356 are defined on the insert plate 350, the retaining members being generally “L” shaped, so as to be slidably received in the retaining grooves 328 or 344 of the spacers 316 or 336, respectively. In the embodiments illustrated in FIGS. 10A-D and 10F, a “shallow” insert plate 350 is depicted, in which the retaining members 356 are defined on the plate ends 352 a, the retaining members 356 extending outwardly from the posterior side 352 c of the plate body 352. When the shallow insert plate 350 is coupled to the spacer 316 (see FIG. 11A), an aperture 322 is defined between the anterior wall 318 a of the spacer body 318 of the spacer 316 and the posterior side 352 c of the plate body 352 of the shallow insert plate. In the embodiment illustrated in FIG. 10E, a “deep” insert plate 350 is depicted, in which the retaining members 356 are defined at the ends of side walls 352 f that extend from the plate ends 352 a, the retaining members 356 extending outwardly from the ends of the side walls 352 f. When the deep insert plate 350 is coupled to the spacer 316, an aperture 322 is defined between the anterior wall 318 a of the spacer body 318 of the spacer 316 and the posterior side 352 c and side walls 352 f of the plate body 352 of the shallow insert plate. The volume of the aperture 322 defined by the spacer 316 coupled to the deep insert plate 350 is greater than the volume of the aperture 322 defined by the spacer 316 coupled to the deep insert plate 350.

Interlocking members can be defined on the coupling members, the interlocking members configured to receive complementary interlocking members, such as the retaining grooves 328 or 344 defined in the spacers 316 or 336, respectively, in releasably locking engagement. For example, in the illustrated embodiments, interlocking members in the form of locking grooves 358 are defined in the ends of the retaining members 356. The locking grooves are define a height in the transverse direction, and are of sufficient height to receive the locking ridges 330 or 346 of the spacers 316 or 336, respectively, therein. In addition to locking the insert plate 350 into position with respect to a spacer 316 or 336, the interlocking members can be configured to facilitate a desired alignment in the transverse direction between the insert plate 350 and the respective spacer, as described above. In the illustrated embodiments the locking grooves 358 can define a height that is longer than the corresponding height of the locking ridges 330 or 346, in order to allow for a limited amount of translation by the insert plate 350 and the respective spacer with respect to each other.

It should be appreciated that the insert plate 350 and spacers 316 and 336 are not limited to the illustrated configurations of the coupling members and/or interlocking members. For example, the retaining grooves 328 or 344 could be defined in the insert plate 350, and the retaining members 356 could be defined on the spacers 316 or 336. Similarly, the locking ridges 330 or 346 could be defined on the retaining members 356, and the locking grooves 358 could be defined in the retaining grooves 328 or 344. It should further be appreciated that the coupling members are not limited to the illustrated structures of the retaining grooves 328 and 344 or the retaining members 356. For example, the respective orientations of the retaining grooves 328 or 344 and the retaining members 356 could be reversed with respect to the lateral direction. It should further still be appreciated that the insert plate 350 and spacers 316 and 336 are not limited to the illustrated coupling members and/or interlocking members, and that any alternative structures can be employed to couple and/or lock the spacers 316 or 336 and the insert plate 350 with respect to each other.

The upper and lower surfaces 352 d-e of the plate body 352 can be configured as bone-engaging surfaces, for example by defining gripping structures thereon, such as teeth, spikes, or the like. The gripping structures can be configured to engage adjacent underlying structures, such as the endplates of adjacent vertebral bodies, when the intervertebral implant 400 is inserted into an intervertebral space. In the embodiments illustrated in FIGS. 10A-D and 10F, portions of the upper and lower surfaces 352 d-e have teeth 360 defined thereon. The teeth 360 may be pyramidal, saw toothed or other similar shapes. In the embodiment illustrated in FIG. 10E, the entireties of the upper and lower surfaces 352 d-e have teeth 360 defined thereon. The upper and lower edges 352 d′-e′ of the upper and lower surfaces 352 d-e, respectively, can be rounded. Rounding the upper and lower edges 352 d′-e′ can facilitate easier insertion and/or removal of the insert plate 350, and thus the intervertebral implant 400, from an intervertebral space, for example by minimizing required distraction of the end plates of adjacent vertebral bodies. Distinct portions, up to an entirety of the upper and lower edges 352 d′-e′ can be rounded using substantially constant or varying radii of curvature.

The geometry of the upper and lower surfaces 352 d-e of the plate body 352 may be defined to generally conform the insert plate 350 to the geometry of the spacers 316 or 336. For example, in the illustrated embodiments, the upper and lower surfaces 352 d-e are defined as partially convex surfaces. In particular, the upper and lower surfaces 352 d-e exhibit lateral convexity in the regions C5 near the plate ends 352 a, the convexity on the upper and lower surfaces 352 d-e being symmetric with respect to each other. The height of the insert plate 350 gradually decreases between the anterior and posterior sides 352 b-c, respectively (see FIGS. 12A-B). It should be appreciated that the insert plate 350 is not limited to the illustrated geometry of the upper and lower surfaces 352 d-e, and that the upper and lower surfaces 352 d-e can be defined with full or partial convexity in the anterior-posterior and/or lateral directions, with full or partial concavity in the anterior-posterior and/or lateral directions, with a combination of partial convexity and concavity in the anterior-posterior and/or lateral directions, or with no curvature at all (i.e., substantially flat) in the anterior-posterior and/or lateral directions. It should further be appreciated that the regions C5 can be defined with wider or narrower widths in the lateral direction. It should further still be appreciated that the geometry of the upper and lower surfaces 352 d-e can be defined either symmetrically or asymmetrically with respect to each other. It should further still be appreciated that the height of the insert plate 350 between the anterior and posterior sides 352 b-c, respectively, may gradually increase, may have a gradual decrease followed by a gradual increase, may have a gradual increase followed by a gradual decrease, or may be generally constant, and that the height between the plate ends 352 a may increase and/or decrease, or may be generally constant.

The anterior side 352 b of the plate body 352 can define a concave recess 362, the recess configured to receive the complementary convex surface of a blocking plate, such as the blocking plate 132 described above. The insert plate 350 can also have a central bore 364 defined therethrough, the central bore 364 defining a threaded inner bore surface 364 a, the threads of the inner bore surface 364 a configured to engage complementary threads of a locking screw, such as the locking screw 138 described above.

The plate body 352 can also have one or more guide apertures 366 defined therethrough, the guide apertures 366 configured to slidably receive bone fixation members therein, such as the arcuate fixation members 12D, and to define insertion trajectories into underlying structures for the fixation members received therein. In the illustrated embodiments, the guide apertures 366 are defined as substantially straight guide apertures extending through the plate body 352 from within the concave recess 362 in the anterior side 352 b through the posterior side 352 c. The guide apertures 366 can have substantially uniform cross sectional geometries that are defined to substantially conform to the cross sectional geometry of the intermediate portion 300 c of the body 300 of the arcuate fixation member 12D.

The guide apertures 366 and/or the arcuate fixation members 12D can be configured to releasably lock respective arcuate fixation members 12D in inserted positions within the guide apertures 366. For example, in the illustrated embodiments, recessed ledges 368 are defined in the surface of the concave recess 362 around a portion of the perimeter of each of the guide apertures 366, the recessed ledges 368 configured to receive the lower surfaces 304 b of the heads 304 of respective arcuate fixation members 12D when the arcuate fixation members 12D are inserted into respective guide apertures 366. One or more surfaces within the recessed ledges 368 can be configured to engage with complementary tapered surfaces defined on the heads 304 of respective arcuate fixation members 12D, for instance surfaces 304 c, thereby locking the arcuate fixation members 12D in respective inserted positions. In an alternative embodiment, the cross sectional geometries of the guide apertures 366 can be tapered between the anterior and posterior sides 352 b-c of the plate body 352, such that the arcuate fixation members 12D are press fit within the guide apertures 366 as they are inserted. Of course the arcuate fixation members 12D and/or the guide apertures 366 can be configured such that no locking affect is imparted therebetween. It should be appreciated that the above-described blocking plate 132 and locking screw 138 can be employed to secure the arcuate fixation members 12D within inserted positions in the guide apertures, whether or not the arcuate fixation members 12D and/or the guide apertures 366 are configured to releasably lock with respect to each other.

The guide apertures 366 can be disposed about the central bore 364 at any desired locations and can define any insertion trajectories as appropriate. In the illustrated embodiments, the guide apertures 366 are defined in opposing quadrants around the central bore 364, with two guide apertures 366 located near the upper surface 352 d and defining two generally outward and cranial insertion trajectories, and two guide apertures 366 located near the lower surface 352 e and defining two generally outward and caudal insertion trajectories. It should be appreciated that the insert plate 350 is not limited to the illustrated configuration of guide aperture 366 locations and insertion trajectories, and that the insert plate 350 can be differently configured with any number of guide apertures 366 defined at any locations on the plate body 352 and having any insertion trajectories. It should further be appreciated that the guide apertures 366 can be straight, curved along one or more locations between the anterior and posterior sides 352 b-c, respectively, or any combination thereof.

Referring now to FIGS. 11A-12C, an example embodiment of an intervertebral implant 400 constructed from components of the intervertebral implant system 100 is illustrated. In particular, the intervertebral implant 400 includes an insert plate 350 coupled to a spacer 316. The intervertebral implant 400 can further include one or more arcuate fixation members 12D, a blocking plate 132, and/or a locking screw 138 (see FIGS. 14A-B), for example in accordance with the insert plate 350 provided. It should be appreciated that the intervertebral implant 400 can be alternatively constructed with the spacer 336, that the insert plate 350 can be provided as a shallow insert plate 350 or a deep insert plate 350 as described above, and that the insert plate 350 can be constructed with or without the guide apertures 366. In the illustrated embodiment, the spacer 316, and in particular the outer wall 318 c, is constructed so that the width W of the spacer 316 in the lateral direction substantially conforms to the width of the insert plate 350 in the lateral direction. The insert plate 350 coupled to the spacer 316 in the illustrated embodiment is a shallow insert plate 350, as described above. When coupled to each other in an assembled configuration, the spacer 316 and the insert plate 350 define a “footprint” of the intervertebral implant 400, the footprint referring to the shape of the outer periphery of the intervertebral implant 400 as defined by the outer wall 318 c of the spacer 316 and the anterior side 352 b of the insert plate 350.

It should be appreciated that the intervertebral implant 400 is not limited to the illustrated footprint, and that the spacer 316 and/or the insert plate 350 can be differently constructed to define alternative footprints of the intervertebral implant 400. For example, the deep insert plate 350, described above, can be coupled to the spacer 316 in lieu of the shallow insert plate 350, defining an intervertebral implant 400 having a larger footprint than the footprint defined by the shallow insert plate 350 coupled to the spacer 316 (see FIG. 12A). Additionally, when the deep insert plate 350 is coupled to the spacer 316, the aperture 322 defined by the anterior wall 318 a of the spacer 316 and the posterior side 352 c of the insert plate 350 is larger than the equivalent aperture 322 defined when the shallow insert plate 350 is coupled to the spacer 316. The spacer 316 can also be differently constructed, for example by defining the outer wall 318 c with alternative widths W of the spacer 316 in the lateral direction and/or depths D of the spacer 316 in the anterior-posterior direction. For instance, the spacer 316 depicted in FIGS. 12B-C has a greater width and depth than the spacer 316 depicted in FIGS. 11A and 12A, thereby defining intervertebral implants 400 with larger footprints when coupled to the shallow or deep insert plates 350, as depicted in FIGS. 12B-C, respectively. It should be appreciated that the spacer 336 can similarly be differently constructed with varying widths and/or depths, thereby defining intervertebral implants 400 with differently sized footprints when coupled to the shallow or deep insert plates 350.

Referring now to FIGS. 13A-B, in addition to providing for the construction of intervertebral implants 400 defining varying footprints, the components of the intervertebral implant system 100 also provide for the construction of intervertebral implants 400 defining varying lordotic angles. The lordotic angle θ of an intervertebral implant 400 can be defined by the geometry of its component parts, such as the surface geometry of the components and/or the height of the components. In the embodiment illustrated in FIG. 13A, a spacer 316 is coupled to an insert plate 350 having a height that is shorter than the height of the spacer 316 at the ends 318 b of the anterior wall 318 a. The lordotic angle θ of the intervertebral implant 400 is defined by the spacer 316. In an alternative embodiment illustrated in FIG. 13B, the spacer 316 is identical to the spacer 316 used in constructing the intervertebral implant 400 depicted in FIG. 13A, but is coupled to an insert plate 350 having a height that is taller than the height of the spacer 316 at the ends 318 b of the anterior wall 318 a. The increased height of the insert plate 350 produces a corresponding increase in the magnitude of the lordotic angle θ of the intervertebral implant 400. It should be appreciated that the lordotic angle defined by intervertebral implants 400 constructed using the spacer 336 can similarly be varied based upon the height of the insert plate 350 coupled thereto. It should further be appreciated that the spacers 316 and/or 336 can be differently constructed with varying heights, thereby defining intervertebral implants 400 with different lordotic angles when coupled to identical insert plates 350.

Referring now to FIGS. 14A-B, an example intervertebral implant 400 is illustrated in an exploded view containing selected components of the intervertebral implant system 100, and in an assembled configuration after being inserted into an intervertebral space, respectively. The characteristics of the assembled intervertebral implant 400, for instance the footprint and/or lordotic angle defined thereby, can be tailored when selecting the individual components, for example in accordance with region of the spine where the intervertebral implant 400 will be inserted, particular patient anatomy, and the like. Thus, the intervertebral implant system 100 can be described as a modular intervertebral implant system 100 that allows a surgeon to construct a patient specific intervertebral implant 400. In the illustrated example, the spacer 316 and insert plate 350 can be selected based upon the desired footprint and/or or lordotic angle that will be defined by the intervertebral implant. The quantity and length of arcuate fixation members 12C and/or 12D can also be selected.

Once the components of the intervertebral implant system 100 have been selected, the spacer can be coupled to the insert plate by inserting the retaining members of the insert plate into the retaining grooves on the spacer and advancing the retaining members until the locking ridges are received in the locking grooves. The intervertebral implant 400 can then be filled with bone growth inducing substances as described above and inserted into an intervertebral space between adjacent vertebral bodies using an insertion, or delivery instrument (not shown). The arcuate fixation members can then be inserted into the guide apertures and driven into place within the adjacent vertebral bodies. Once the arcuate fixation members are inserted, a blocking plate can be disposed into the concave recess in the insert plate and a locking screw can be driven through the blocking plate and into the insert plate, thereby securing the intervertebral implant in an assembled and inserted configuration.

It should be appreciated that a variety of kits can be provided that contain one or more components of the intervertebral implant system 100. The components of the kits may be configured the same or differently. For example, within a single kit, arcuate fixation members 12C and/or 12D may be provided that have different lengths, different radii of curvature, differing head configurations, differing cross sectional geometries, and so on, depending for example on the type of procedure being performed by a surgeon, or on the particular anatomies of individual patients. The kits may also be configured differently with respect to which components of the intervertebral implant system 100 are included in the kits. For example, a kit for the intervertebral implant system 100 may include arcuate fixation members 12C and/or 12D of different lengths, radii of curvature, and/or features, and may include one or more of spacers 108, 316 and/or 336 having different heights, perimeter geometries, or surface geometries, or defining different lordotic angles, insert plates 116 or 350 having different heights, perimeter geometries, surface geometries, and guide apertures, blocking plates 132, or locking screws 138.

Although arcuate fixation members and the other components of the intervertebral implant system 100 have been described herein with reference to preferred embodiments or preferred methods, it should be understood that the words which have been used herein are words of description and illustration, rather than words of limitation. For example, it should be noted that although the intervertebral implant system 100 has been described herein with reference to particular structure, methods, and/or embodiments, the scope of the instant disclosure is not intended to be limited to those particulars, but rather is meant to extend to all structures, methods, and/or uses of the intervertebral implant system 100. Those skilled in the relevant art, having the benefit of the teachings of this specification, may effect numerous modifications to the intervertebral implant system 100 as described herein, and changes may be made without departing from the scope and spirit of the instant disclosure, for instance as recited in the appended claims. 

What is claimed:
 1. An intervertebral implant kit comprising: a plurality of spacer bodies, at least a pair of the spacer bodies defining a different at least one of a size and shape; a plurality of inserts, at least one of the inserts configured to be coupled to any of the plurality of spacer bodies, each insert defining at least one guide aperture that extends therethrough; and a plurality of curved fixation members each configured for insertion at least partially through the at least one guide aperture, each curved fixation member defining a proximal end, a distal end spaced from the proximal end along a central axis, and a curved fixation body extending along the central axis, the curved fixation body defining a cross-sectional shape that conforms to the at least one guide aperture such that the curved fixation body is rotatably fixed in the at least one guide aperture when inserted in the at least one guide aperture, the distal end defining a tapered tip that extends distally from the curved fixation body, the tapered tip configured to cut into a vertebral body.
 2. The intervertebral implant kit as recited in claim 1, wherein the at least two of the plurality of spacer bodies define different lordotic angles.
 3. The intervertebral implant kit as recited in claim 1, wherein at least one of the plurality of inserts has a height different from that of at least a portion of one of the plurality of spacer bodies.
 4. The intervertebral implant kit as recited in claim 1, wherein a height of the at least one of the plurality of inserts is greater than that of a second one of the plurality of inserts.
 5. The intervertebral implant kit as recited in claim 1, wherein at least one of the plurality of inserts defines a pair of side walls that extend from opposing ends of the plate.
 6. The intervertebral implant kit as recited in claim 1, wherein when at least one of the plurality of curved fixation members is inserted through the at least one guide aperture, the tapered tip and the curved fixation body translate through the at least one guide aperture.
 7. The intervertebral implant kit as recited in claim 1, wherein a portion of at least one of the plurality of spacers has a height different from that of a corresponding portion of a second one of the plurality of spacers.
 8. The intervertebral implant kit as recited in claim 1, wherein at least one of the plurality of spacers defines a perimeter that is different from that defined by a second one of the plurality of spacers.
 9. An intervertebral implant comprising: a spacer body; an insert configured to be coupled the spacer body, the insert defining a plurality of guide apertures extending therethrough; and a bone fixation member configured to be inserted at least partially through the at least one of the plurality of guide apertures and at least partially into a vertebral body, the bone fixation member defining a proximal end and a distal end spaced from the proximal end along a central axis, the bone fixation member, comprising: a fixation body having a curved intermediate portion extending between the proximal and distal ends, the curved intermediate portion defining a cross-sectional shape that conforms with the at least one of the plurality of guide apertures such that the bone fixation member is rotatably fixed in the at least one guide aperture during insertion therethrough, and a tapered tip distal to the curved intermediate portion and extending distally from the fixation body, the tapered tip configured to cut into bone.
 10. The intervertebral implant as recited in claim 9 wherein the bone fixation member further comprises a guidance member disposed at least partially on the tip, the guidance member configured to guide the bone fixation member along an insertion trajectory as the bone fixation member is inserted into the vertebral body.
 11. The intervertebral implant as recited in claim 10, wherein the guidance member comprises a flute defined by the tip, the flute extending substantially parallel to the insertion trajectory.
 12. The intervertebral implant as recited in claim 11, wherein the guidance member comprises a plurality of flutes defined by the tip.
 13. The intervertebral implant as recited in claim 12, wherein the flutes extend substantially parallel to each other.
 14. The intervertebral implant as recited in claim 10, wherein the guidance member comprises a projection that protrudes from the tip.
 15. The intervertebral implant as recited in claim 14, wherein the projection comprise a keel.
 16. The intervertebral implant as recited in claim 15, wherein the guidance member further comprises at least one wing disposed adjacent the keel, such that a flute is disposed between the keel and the at least one wing.
 17. The intervertebral implant as recited in claim 16, wherein the guidance member further comprises a second wing disposed adjacent the keel, such that the keel is disposed between the wings.
 18. The intervertebral implant as recited in claim 17, wherein flutes are defined between the keel and each of the respective wings.
 19. The intervertebral implant as recited in claim 17, wherein the keel is substantially centrally disposed between the wings.
 20. The intervertebral implant as recited in claim 14, wherein the guidance member comprises at least one offset wing.
 21. The intervertebral implant as recited in claim 20, wherein the guidance member further comprises a pair of offset wings.
 22. The intervertebral implant as recited in claim 21, wherein the guidance member further comprises a keel disposed between the wings.
 23. The intervertebral implant as recited in claim 22, further defining a pair of flutes disposed between the wings and the keel.
 24. The intervertebral implant as recited in claim 10, wherein the guidance member terminates proximal of the tip in the intermediate portion of the body.
 25. The intervertebral implant as recited in claim 10, wherein the body includes a gripping structure configured to be retain the fixation member in an inserted position within the vertebral body.
 26. The intervertebral implant as recited in claim 25, wherein the gripping structure comprises a plurality of teeth defined in the intermediate portion of the body.
 27. The intervertebral implant as recited in claim 26, wherein the plurality of teeth are defined in rows on opposing sides of the intermediate portion of the body.
 28. The intervertebral implant as recited in claim 9, wherein the spacer body defines an upper bone-engaging surface, a lower bone-engaging surface spaced apart from the upper bone-engaging surface, an outer wall defining a posterior wall, an anterior wall opposite the posterior wall, and a pair of side walls that extend between the posterior wall and the anterior wall, the side walls being spaced apart from each other along a first direction, and the anterior and posterior walls being spaced from each other along a second direction that is perpendicular to the first direction, the outer wall at least partially defining a pair of apertures that each extends through the upper and lower bone-engaging surfaces at a location between the posterior and anterior walls, the spacer body further including an inner wall that separates one of the pair of apertures from the other of the pair of apertures.
 29. The intervertebral implant as recited in claim 28, wherein the spacer body defines at least one opening that extends through the inner wall separates the pair of apertures.
 30. The intervertebral implant as recited in claim 28, wherein the spacer body defines a pair of openings extending through the anterior wall so as to place the pair of apertures in communication with the second aperture.
 31. An intervertebral implant comprising: a spacer body configured to be implanted into an intervertebral space, the spacer body defining an upper bone-engaging surface, a lower bone-engaging surface spaced apart from the upper bone-engaging surface, an outer wall defining a posterior wall, an anterior wall opposite the posterior wall, and a pair of side walls that extend between the posterior wall and the anterior wall, the side walls being spaced apart from each other along a first direction, and the anterior and posterior walls being spaced from each other along a second direction that is perpendicular to the first direction, the outer wall extending from the upper bone-engaging surface to the lower bone-engaging surface, the outer wall at least partially defining a pair of apertures that each extends through the upper and lower bone-engaging surfaces at a location between the posterior and anterior walls, the spacer body further including an inner wall that separates one of the pair of apertures from the other of the pair of apertures; an insert configured to be coupled to the spacer body, the insert defining a plate, wherein the insert and the anterior wall of the spacer body define a second aperture therebetween, the second aperture being aligned with the inner wall along the second direction, the insert further defining at least one guide aperture extending therethrough, the at least one guide aperture configured to receive a curved bone fixation member.
 32. The intervertebral implant as recited in claim 31, further comprising at least one curved bone fixation member configured to be inserted at least partially through the at least one guide aperture, the at least one curved fixation member defining a cross-sectional shape that conforms to the at least one guide aperture such that the at least one curved fixation member is rotatably fixed in the at least one guide aperture during insertion therethrough.
 33. The intervertebral implant as recited in claim 31, wherein at least a portion of the upper and lower bone-engaging surfaces have relief grooves defined therein, the relief grooves configured to partially receive respective curved fixation members therein.
 34. The intervertebral implant as recited in claim 32, wherein the spacer body and the insert define respective upper and lower bone-engaging surfaces, at least a portion of the respective upper and lower bone-engaging surfaces having a plurality of gripping structures defined thereon, the gripping structures configured to engage adjacent vertebral bodies when the intervertebral implant is inserted into an intervertebral space.
 35. The intervertebral implant as recited in claim 31, wherein the outer wall defines an enclosed perimeter of the spacer body.
 36. The intervertebral implant as recited in claim 32, wherein the at least one guide aperture extends substantially straight and the curved bone fixation member is curved.
 37. The intervertebral implant as recited in claim 31, wherein the outer wall defines an inner surface that defines at least one cavity therein.
 38. The intervertebral implant as recited in claim 37, wherein the at least one cavity is open at least one of the pair of apertures.
 39. The intervertebral implant as recited in claim 31, wherein the spacer body defines at least one opening extending through the outer wall.
 40. The intervertebral implant as recited in claim 31 wherein the spacer body defines at least one opening that extends through the inner wall that separates the pair of apertures.
 41. The intervertebral implant as recited in claim 31, wherein the spacer body defines a pair of openings extending through the anterior wall so as to place the pair of apertures in communication with the second aperture.
 42. The intervertebral implant as recited in claim 31, wherein the an anterior wall faces the plate, and at least a portion of the anterior wall is curved away from the plate when the insert is coupled to the spacer body.
 43. The intervertebral implant as recited in claim 31, wherein the insert has a height different from that of at least a portion of the spacer body.
 44. The intervertebral implant as recited in claim 43, wherein the height of the insert is taller than that of the at least a portion of the spacer body so that a lordotic angle defined by the intervertebral implant is greater than that defined by the spacer body.
 45. The intervertebral implant as recited in claim 31, wherein each of the insert and the spacer body further comprises respective interlocking members configured to secure the insert to the spacer body when the insert is coupled to the spacer body.
 46. The intervertebral implant as recited in claim 31, wherein the at least one curved fixation member has a length greater than a length of the at least one guide aperture, and a tip configured to cut into a vertebral body as the tip is driven through the at least one guide aperture and into the vertebral body.
 47. An intervertebral implant comprising: a hollow spacer body configured to be implanted into an intervertebral space, the spacer body having upper and lower plates, a hollow region disposed between the upper and lower plates, and an outer wall extending between the upper and lower plates, wherein the spacer body defines a plurality of apertures extending through each of the upper and lower plates and into the hollow region; an insert configured to be coupled to the spacer body, the insert defining a plate, wherein the insert is disposed opposite at least a portion of the outer wall, the insert further defining at least one guide aperture extending therethrough, the at least one guide aperture configured to receive a bone fixation member; and at least one curved fixation member configured to be inserted at least partially through the at least one guide aperture.
 48. The intervertebral implant as recited in claim 47, further comprising a curved bone fixation member configured to be inserted at least partially through the at least one aperture, wherein the least one curved fixation member defines a cross- sectional shape that conforms with the at least one guide aperture such that the at least one curved fixation member is rotatably fixed in the at least one guide aperture during insertion therethrough.
 49. The intervertebral implant as recited in claim 47, wherein the apertures that extend through the upper plate are aligned with the apertures that extend through the lower plate.
 50. The intervertebral implant as recited in claim 47, wherein that outer wall defines at least a posterior end of the spacer body, and that the spacer body defines an open anterior end that is opposite the posterior end.
 51. The intervertebral implant as recited in claim 50, wherein the open anterior end is disposed between the posterior end and the insert.
 52. The intervertebral implant as recited in claim 47, wherein the at least one guide aperture extends substantially straight and the bone fixation member is curved.
 53. The intervertebral implant as recited in claim 47, wherein the spacer body defines a plurality of slots that extend through the outer wall.
 54. The intervertebral implant as recited in claim 53, wherein the slots are elongate along a direction between the upper and lower plates.
 55. The intervertebral implant as recited in claim 47, wherein the upper and lower plates define respective bone-engaging surfaces.
 56. The intervertebral implant as recited in claim 47, wherein the spacer body and the insert define respective upper and lower bone-engaging surfaces, at least a portion of the respective upper and lower bone-engaging surfaces having a plurality of gripping structures defined thereon, the gripping structures configured to engage adjacent vertebral bodies when the intervertebral implant is inserted into an intervertebral space.
 57. The intervertebral implant as recited in claim 47, wherein the insert defines a height that is different from that of at least a portion of the spacer body.
 58. The intervertebral implant as recited in claim 57, wherein the height of the insert is taller than that of the at least a portion of the spacer body so that a lordotic angle defined by the intervertebral implant is greater than that defined by the spacer body.
 59. The intervertebral implant as recited in claim 47, wherein each of the insert and the spacer body further comprises respective interlocking members configured to secure the insert to the spacer member when the insert is coupled to the spacer member.
 60. The intervertebral implant as recited in claim 47, wherein the at least one curved fixation member has a tip configured to cut into a vertebral body, and the at least one curved fixation member has a length greater than a length of the at least one guide aperture such that the tip can be driven at least partially through the at least one guide aperture and at least partially into the vertebral body. 